Evidence map›Paper›PMID 35095995›Full record

ArticleFrontiers in genetics2021

Whole Blood Transcriptome Analysis in Children with Sickle Cell Anemia.

Beatrice E Gee, Andrea Pearson, Iris Buchanan-Perry, Roger P Simon, David R Archer, Robert Meller

Open access · goldAbstract read
In one paragraph

Article in Frontiers in genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.8field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 13 citations in OpenAlex.

  1. Whole Blood Transcriptomic Analysis of Sickle Cell Trait.European journal of haematology · 2026
    Article
  2. Review
  3. Review
  4. Article
  5. Transcriptional regulators of fetal hemoglobin.Hematology, transfusion and cell therapy · 2024
    Review
  6. Article
  7. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 4 institutions in 1 country.

Beatrice E GeeDepartment of Pediatrics, Morehouse School of Medicine, Atlanta, GA, United States.
Andrea PearsonTranslational Stroke Program, Neuroscience Institute, Morehouse School of Medicine, Atlanta, GA, United States.
Iris Buchanan-PerryDepartment of Pediatrics, Morehouse School of Medicine, Atlanta, GA, United States.
Roger P SimonTranslational Stroke Program, Neuroscience Institute, Morehouse School of Medicine, Atlanta, GA, United States.
David R ArcherAflac Cancer and Blood Disorders Center of Emory University and Children's Healthcare of Atlanta, Atlanta, GA, United States.
Robert MellerTranslational Stroke Program, Neuroscience Institute, Morehouse School of Medicine, Atlanta, GA, United States.
Morehouse School of Medicine · USAflac (United States) · USChildren's Healthcare of Atlanta · USGrady Memorial Hospital · US

Funding

Morehouse School of Medicine Center of Excellence Research Endowment ProgramS21MD000101 · NIMHD · MOREHOUSE SCHOOL OF MEDICINE · PI MONTGOMERY-RICE, VALERIE C. · 2001 to 2015
$74.3M
Research Desogn and Biostatistics CoreU54MD007588 · NIMHD · MOREHOUSE SCHOOL OF MEDICINE · PI HENRY-AKINTOBI, TABIA · 2012 to 2018
$24.8M
Blood transcriptomics as CT adjuvant to exclude hemorrhage in acute strokeR01NS112422 · NINDS · MOREHOUSE SCHOOL OF MEDICINE · PI MELLER, ROBERT · 2020 to 2024
$2.8M
Mechanisms of ASIC-mediated neuronal injuryR01NS104349 · NINDS · MOREHOUSE SCHOOL OF MEDICINE · PI SIMON, ROGER PANCOAST · 2018 to 2023
$1.6M
NIMHD NIH HHS S21 MD000101NIMHD NIH HHS U54 MD007588NINDS NIH HHS R01 NS104349NINDS NIH HHS R01 NS112422
6 · The paper itself

Abstract

Whole transcriptome RNA-sequencing was performed to quantify RNA expression changes in whole blood samples collected from steady state sickle cell anemia (SCA) and control subjects. Pediatric SCA and control subjects were recruited from Atlanta (GA)-based hospital(s) systems and consented for RNA sequencing. RNA sequencing was performed on an Ion Torrent S5 sequencer, using the Ion Total RNA-seq v2 protocol. Data were aligned to the hg19 reference genome and analyzed in the Partek Genomics studio package (v7.0). 223 genes were differentially expressed between SCA and controls (± 1.5 fold change FDR

Indexed as

eQTL analysispathway analysisRNA-sequencingsickle cell diseasetranscriptome

Identifiers

PMID35095995
PMCPMC8793691
OpenAlexW4206374555

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.